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3 rmination, because s.c. inoculation with the capsulated bacillus forms also required toxin synthesis
5 to the pathogenesis of and immunity to other capsulated bacteria, and has contributed to the developm
6 rent directions of galvanotaxis of rough (or capsulate) bacteria and of smooth bacteria are explicabl
7 -derived macrophages was investigated with a capsulate case isolate and an isogenic Tn916-derived non
9 in vitro against SP-A- and SP-B(N)-resistant capsulated Klebsiella pneumoniae (serotype K2) at neutra
12 ctose led to attenuation of bone loss in the capsulated mixed infection and to intensification of bon
13 tion, Fn evaded phagocytosis, whereas in the capsulated mixed infection Pg displayed a greater capaci
15 s were randomly selected for the placebo and capsulated mustard intervention; 9 of 11 subjects receiv
19 ed a truncated or nonsialylated LOS, whether capsulated or not, were more sensitive to the inhibitory
20 enditure did not increase after ingestion of capsulated or uncapsulated mustard compared with placebo
21 of lysosomes with phagosomes containing the capsulate organism was significantly reduced 10 and 30 m
22 these vaccines, along with studies of other capsulated pathogens, should allow the rapid inclusion o
25 sulated mustard or uncapsulated mustard or a capsulated placebo mixture, measurements of energy expen
29 and decreased CR3-dependent clearance of Vi capsulated S. Typhi from the livers and spleens of mice.
33 he novel nanoparticles of DGL-PEG/dermorphin capsulated siRNA (OATP2B1) were applied to deliver siRNA
34 ive disulfide bond, while TET was physically capsulated spontaneously for the aim to suppress P-gp in
39 fections containing Fn and non-capsulated or capsulated strains of Pg were compared with the same inf
42 have recently shown that numerous strains of capsulate (typeable) and acapsulate (non-typeable) H. in
44 nonencapsulated, avirulent pneumococci into capsulated, virulent strains during infection in mice.
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